Informations sur le produit
- GILGFVFTL-acidH-Gly-Ile-Leu-Gly-Phe-Val-Phe-Thr-Leu-OHHLA-A*02:01 Influenza M1 peptideInfluenza Matrix Protein M1 (58 - 66)CEF1 M158-66 matrix protein epitopeGILGFVFTLInfluenza M Matrix1 (58-66) (HLA-A2)
- Matrix Protein M1 (58-66) (Influenza A Virus)
- H2N-Gilgfvftl-Oh
- Gly-Ile-Leu-Gly-Phe-Val-Phe-Thr-Leu
- Influenza Matrix Peptide
- Influenza Matrix Protein M1 (58-66)
- Influenza Virus Matrix Protein (58-66)
- Gilgfvftl
T cell epitopes are presented on the surface of antigen-presenting cells by major histocompatibility complex (MHC) molecules. T cell epitopes presented by MHC class I molecules are typically peptides between 8 and 11 amino acids in length and exhibit MHC-specific sequence motifs. These antigenic peptides are derived from non-structural and structural proteins through proteolysis in the cytosolic compartment. Peptide-MHC-I complexes are then transported to the cell surface of antigen presenting cells and are recognised by CD8+ cytotoxic T lymphocytes (CTL).The interaction between TCL cell receptors and MHC-I induces the differentiation of CTLs. Activated CTLs lyse infected cells, secrete cytokines, and proliferate. This mechanism ensures that cells infected by viruses or intracellular bacteria or cancer cells can be detected.The genes of MHC I and II molecules are polymorphic- each MHC allele has a distinct peptide binding motif which favours certain amino acid anchor residues at defined sequence positions.
Propriétés chimiques
Question d’ordre technique sur : 3D-CRB1001165 Flu mp 58
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